The development of Bruton's tyrosine kinase (BTK) inhibitors from 2012 to 2017: A mini-review-Reference-Cited by-同舟云学术

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The development of Bruton's tyrosine kinase (BTK) inhibitors from 2012 to 2017: A mini-review

Published:2018-05 Issue: Volume:151 Page:315-326
ISSN:0223-5234
Container-title:European Journal of Medicinal Chemistry
language:en
Short-container-title:European Journal of Medicinal Chemistry

Author:

Liang Chengyuan,Tian Danni,Ren Xiaodong,Ding Shunjun,Jia Minyi,Xin Minhang,Thareja Suresh

Funder

National Natural Science Foundation of China

China Postdoctoral Science Foundation

Shaanxi Postdoctoral Science Foundation

Basic Research Plan of the Education Department of Shaanxi Province

Innovative Entrepreneurial Training Program

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Pharmacology,General Medicine

Reference110 articles.

1. Abstract 2599: discovery and pharmacological characterization of the second generation of Btk inhibitors with improved target selectivity and enhanced in vivo efficacy;Zhang;Canc. Res.,2015

2. Structure-activity relationship investigation for benzonaphthyridinone derivatives as novel potent Bruton's tyrosine kinase (BTK) irreversible inhibitors;Wang;Eur. J. Med. Chem.,2017

3. Bruton tyrosine kinase (BTK) and its role in B-cell malignancy;Buggy;Int. Rev. Immunol.,2012

4. Small chemicals with inhibitory effects on PtdIns(3,4,5)P 3 binding of Btk PH domain;Yoon;Bioorg. Med. Chem. Lett.,2014

5. Computational analysis of the binding specificities of PH domains;Jiang;BioMed Res. Int.,2015

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2. Discovery of New Non-covalent Reversible BTK Inhibitors: Synthesis, in silico Studies, and in vitro Evaluations;Chemico-Biological Interactions;2024-09

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